Article: Building a Community Health Center Data Warehouse to Promote Patient-Centered Research in the Asian American, Native Hawaiian, and Pacific Islanders Population

“Building a Community Health Center Data Warehouse to Promote Patient-Centered Research in the Asian American, Native Hawaiian, and Pacific Islanders Population”
Volume 12:1-2, p. 21 (2014)
by Vivian Li, Rosy Chang Weir, Thu Quach, Suzanne Gillespie, Mary Ann McBurnie, Ady Oster, Reesa Laws, Kari Alperovitz-Bichell, Erin O’Brien Kaleba and Christine Nelson

ABSTRACT: In 2010, the Health Resources and Services Administration (HRSA) established the Community Health Applied Research Net- work (CHARN) to build research infrastructure and capacity at community health centers (CHCs) and to promote comparative effectiveness research in these safety-net settings. A data warehouse with standardized data was created to capture, manage, and share patient-level data with all eighteen participating CHCs, including four CHCs primarily serving Asian American, Native Hawaiian, and Other Pacific Islanders (AANHOPI). AANHOPI patients face unique health risks, yet these large and diverse populations are historically understudied. The CHARN data warehouse provides important opportunities for understanding the health needs of this heterogeneous population.

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Article Citation:
Vivian Li, Rosy Chang Weir, Thu Quach, Suzanne Gillespie, Mary Ann McBurnie, Ady Oster, Reesa Laws, Kari Alperovitz-Bichell, Erin O’Brien Kaleba, and Christine Nelson (2014) Building a Community Health Center Data Warehouse to Promote Patient-Centered Research in the Asian American, Native Hawaiian, and Pacific Islanders Population. AAPI Nexus: Policy, Practice and Community: 2014, Vol. 12, No. 1-2, pp. 21-43.

https://doi.org/10.17953/appc.12.1-2.q388658g01kh7552

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